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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Transition from Childhood to Adulthood in Patients with Duchenne Muscular Dystrophy
Eliza Wasilewska, Sylwia Małgorzewicz, Agnieszka Sobierajska-Rek, et al.
Medicina (2020) Vol. 56, Iss. 9, pp. 426-426
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: an international Delphi consensus study
Diana Castro, Thomas Sejersen, Luca Bello, et al.
European Journal of Paediatric Neurology (2025) Vol. 54, pp. 130-139
Closed Access | Times Cited: 1
Early Cardiac Dysfunction in Duchenne Muscular Dystrophy: A Case Report and Literature Update
Maria Lupu, Irina Pintilie, Raluca Ioana Teleanu, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1685-1685
Open Access | Times Cited: 1
Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids
Marianela Schiava, Robert Muni Lofra, John Bourke, et al.
European Journal of Neurology (2024) Vol. 31, Iss. 6
Open Access | Times Cited: 7
Navigating adulthood: Exploring the transition needs of adolescents and young adults affected by Duchenne or Becker muscular dystrophy
Sharon Barak, Shlomi Laufer, Michal Gudinsky Elyashiv, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0317006-e0317006
Open Access
Lower-Limb Orthoses in Duchenne Muscular Dystrophy
Gizem Peken Avcı, Özge İpek Dongaz, Banu Bayar
JPO Journal of Prosthetics and Orthotics (2025) Vol. 37, Iss. 1, pp. e1-e5
Closed Access
A Formal Needs Assessment in Palliative Care Clinic Development for Adolescent/Young Adults (AYAs) with Neuromuscular Disease
Taylor Jersak, Loren Steinfeldt, Kelstan Ellis, et al.
Journal of Pain and Symptom Management (2025)
Closed Access
Lost in Transition: Challenges in the Journey from Pediatric to Adult Care for a Romanian DMD Patient
Maria Lupu, Maria-Alexandra Marcu, Diana Epure, et al.
Healthcare (2025) Vol. 13, Iss. 7, pp. 830-830
Open Access
Recomendaciones de prescripción de ayudas técnicas en la rehabilitación de pacientes con distrofia muscular de Duchenne
Sandra Milena Castellar-Leones, Edicson Ruiz Ospina, Miguel Ángel Gutiérrez-Ramírez, et al.
Revista Ciencias de la Salud (2025) Vol. 23, Iss. Especial, pp. 1-19
Open Access
Recomendaciones de expertos para la transición a la vida adulta del paciente con distrofia muscular de Duchenne
Edna Julieth Bobadilla-Quesada, Manuel Huertas-Quiñones, Juan David Lasprilla Tovar, et al.
Revista Ciencias de la Salud (2025) Vol. 23, Iss. Especial, pp. 1-30
Open Access
Respiratory Telerehabilitation of Boys and Young Men with Duchenne Muscular Dystrophy in the COVID-19 Pandemic
Agnieszka Sobierajska-Rek, Łukasz Mański, Joanna Jabłońska-Brudło, et al.
International Journal of Environmental Research and Public Health (2021) Vol. 18, Iss. 12, pp. 6179-6179
Open Access | Times Cited: 22
Human Dystrophin Expressing Chimeric (DEC) Cell Therapy Ameliorates Cardiac, Respiratory, and Skeletal Muscle's Function in Duchenne Muscular Dystrophy
Maria Siemionow, Paulina Langa, Michał Harasymczuk, et al.
Stem Cells Translational Medicine (2021) Vol. 10, Iss. 10, pp. 1406-1418
Open Access | Times Cited: 22
Outcome Measures in Duchenne Muscular Dystrophy
Silvia Benemei, Francesca Gatto, Luca Boni, et al.
Acta Neurologica Belgica (2024)
Open Access | Times Cited: 2
The Importance of Implementing a Transition Strategy for Patients with Muscular Dystrophy: From Child to Adult—Insights from a Tertiary Centre for Rare Neurological Diseases
Maria Alina Lupu, Mihaela Roxana Ioghen, Radu‐Ștefan Perjoc, et al.
Children (2023) Vol. 10, Iss. 6, pp. 959-959
Open Access | Times Cited: 4
Quality of life and caregiving burden associated with parenting a person with Duchenne/Becker muscular dystrophy in Poland
Jan Domaradzki, Dariusz Walkowiak
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 1
Is It Possible to Have Home E-Monitoring of Pulmonary Function in Our Patients with Duchenne Muscular Dystrophy in the COVID-19 Pandemic?—A One Center Pilot Study
Eliza Wasilewska, Agnieszka Sobierajska-Rek, Sylwia Małgorzewicz, et al.
International Journal of Environmental Research and Public Health (2021) Vol. 18, Iss. 17, pp. 8967-8967
Open Access | Times Cited: 10
The Association between the Respiratory System and Upper Limb Strength in Males with Duchenne Muscular Dystrophy: A New Field for Intervention?
Agnieszka Sobierajska-Rek, Eliza Wasilewska, Karolina Śledzińska, et al.
International Journal of Environmental Research and Public Health (2022) Vol. 19, Iss. 23, pp. 15675-15675
Open Access | Times Cited: 6
Neuromuscular disorders and transition from pediatric to adult care in a multidisciplinary perspective: a narrative review of the scientific evidence and current debate.
Giuseppe Accogli, Camilla Ferrante, Isabella Fanizza, et al.
PubMed (2022) Vol. 41, Iss. 4, pp. 188-200
Closed Access | Times Cited: 3
Nutritional Issues among Children with Duchenne Muscular Dystrophy—Incidence of Deficiency and Excess Body Mass
Edyta Wernio, Eliza Wasilewska, Sylwia Czaja-Stolc, et al.
Nutrients (2024) Vol. 16, Iss. 13, pp. 2143-2143
Open Access
Essential components of an effective transition from paediatric to adult neurologist care for adolescents with Duchenne muscular dystrophy; a consensus derived using the Delphi methodology in Eastern Europe, Greece and Israel
Mária Judit Molnár, Léna Szabó, Oana Aurelia Vladâcenco, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Psychometric evaluation of the PROMIS parent proxy mobility item bank for use in Duchenne muscular dystrophy
Linda Lowes, Corinne M. Le Reun, Lindsay N. Alfano, et al.
Developmental Medicine & Child Neurology (2024)
Open Access
Development and Economic Evaluation of a Patient-Centered Care Model for Children With Duchenne Muscular Dystrophy: Protocol for a Quasi-Experimental Study
Titiksha Sirari, Renu Suthar, Amarjeet Singh, et al.
JMIR Research Protocols (2023) Vol. 12, pp. e42491-e42491
Open Access | Times Cited: 1
Surveying Therapists on Seating Approaches for Patients with Muscular Dystrophy in Japan
Hitomi Fujita, Atsushi Tsukada, Tomoko Ohura
Healthcare (2021) Vol. 9, Iss. 6, pp. 631-631
Open Access | Times Cited: 1
Transition von langzeitbeatmeten Kindern in die Erwachsenenmedizin
Kurt H. Wollinsky, Hans Fuchs, B. Schönhofer
Pneumologie (2023) Vol. 77, Iss. 08, pp. 554-561
Closed Access
Essential components of an effective transition from paediatric to adult neurologist care for adolescents with Duchenne muscular dystrophy; a consensus derived using the Delphi methodology in Eastern Europe, Greece and Israel
Mária Judit Molnár, Léna Szabó, Oana Aurelia Vladâcenco, et al.
Research Square (Research Square) (2023)
Open Access
Tele-Rehabilitation for Boys with Duchenne Muscular Dystrophy in India Amidst the COVID-19 Pandemic: An Implementation Study
Priyanka Gupta, Amrit Pal Singh Sood, Seveka Bali, et al.
International Journal of Disabilities Sports & Health Sciences (2023) Vol. 7, Iss. 1, pp. 13-20
Open Access
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